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Titlebook: Cell Cycle Deregulation in Cancer; Greg H. Enders Book 2010 Springer Science+Business Media, LLC 2010 DNA.biology.cancer.cancer therapy.ce

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發(fā)表于 2025-3-21 17:29:35 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱Cell Cycle Deregulation in Cancer
編輯Greg H. Enders
視頻videohttp://file.papertrans.cn/223/222787/222787.mp4
概述outlines major cell cycle perturbations that drive tumorigenesis and considers the prospects for using such knowledge in cancer therapy..Includes supplementary material:
叢書(shū)名稱Current Cancer Research
圖書(shū)封面Titlebook: Cell Cycle Deregulation in Cancer;  Greg H. Enders Book 2010 Springer Science+Business Media, LLC 2010 DNA.biology.cancer.cancer therapy.ce
描述.Cancer is fundamentally a disease of abnormal cell proliferation: Cancer cells multiply when and where they should not. This proliferation entails escape from normal bounds imposed by the tissue environment, the internal biology of the cell (DNA damage, chromosomal imbalances, disorganized mitotic spindles), and the proliferative history of the cell (normal generational times). Some of the key oncogenic events in cancer directly perturb proteins that regulate progression through the cell division cycle, others alter cell cycle progression indirectly, through effects on signaling pathway that impinge on the cell cycle. This biology is fundamentally important in cancer therapy. Many of the workhorse treatments for cancer rely on killing proliferating cells. Furthermore, there is growing recognition that stem cell-transit amplifying cell hierarchies may persist or be generated during tumorigenesis, generating important functional heterogeneity in cell cycle control among tumor cells, with far-reaching scientific and clinical implications. This volume outlines major cell cycle perturbations that drive tumorigenesis and considers the prospects for using such knowledge in cancer therapy
出版日期Book 2010
關(guān)鍵詞DNA; biology; cancer; cancer therapy; cell; esophagus; research; senescence; tumor; tumorigenesis
版次1
doihttps://doi.org/10.1007/978-1-4419-1770-6
isbn_softcover978-1-4614-2569-4
isbn_ebook978-1-4419-1770-6Series ISSN 2199-2584 Series E-ISSN 2199-2592
issn_series 2199-2584
copyrightSpringer Science+Business Media, LLC 2010
The information of publication is updating

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https://doi.org/10.1007/978-94-017-6766-8feration is a fundamental feature of all types of cancer. One of the key regulators of cell proliferation is the E2F transcription factor. E2F controls the expression of many genes that are required for cells to divide and elevated E2F activity is found in most tumor cells. The activation and inacti
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https://doi.org/10.1007/978-94-017-6766-8tiation of DNA replication, and virtually all components of the pre-RC are regulated by complex mechanisms that center around the activity of cyclin-dependent kinases (CDKs). CDK/cyclin complexes both positively and negatively regulate pre-RC components, including their expression, activity, stabili
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The Essence of Acts of Empathy,apoptosis. Recently, both of these proteins were found to be intimately tied to metabolic pathways and to play surprising roles in autophagy. Autophagy (“self-eating”) is a critical response of eukaryotic cells to stress. During this process, portions of the cytosol, including cytoplasmic organelles
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https://doi.org/10.1007/978-94-017-7402-4 the biological organization of tumours. These cells, named tumour-initiating cells (TICs), or cancer stem cells (CSCs), share phenotypic and functional characteristics with normal stem cells, most notably their ability to self-renew. Here we discuss regulation of self-renewal in normal haematopoiet
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https://doi.org/10.1007/978-94-017-9984-3rogression to fully fledged cancer would allow for chemoprevention or therapeutic interventions; however in most cases, IEN remains undetected and the exact mechanisms for progression remain unknown. Barrett’s oesophagus, the premalignant stage of oesophageal adenocarcinoma, is the perfect model to
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